"57955-0275-2" National Drug Code (NDC)

NDC Code	57955-0275-2
Package Description	59 mL in 1 BOTTLE, SPRAY (57955-0275-2)
Product NDC	57955-0275
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Tinnitus Relief
Non-Proprietary Name	Arnica Montana, Calcarea Carbonica, Chenopodium Anthelminticum, Chininum Salicylicum, Cimicifuga Racemosa, Coffea Tosta, Kali Iodatum, Kalmia Latifolia, Magnesia Carbonica, Manganum Aceticum, Manganum Carbonicum, Mercurius Vivus, Natrum Salicylicum, Salicylicum Acidum, Thiosinaminum, Thyroidinum
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20121106
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	King Bio Inc.
Substance Name	ARNICA MONTANA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; DYSPHANIA AMBROSIOIDES; QUININE SALICYLATE; BLACK COHOSH; COFFEA ARABICA SEED, ROASTED; POTASSIUM IODIDE; KALMIA LATIFOLIA LEAF; MAGNESIUM CARBONATE; MANGANESE ACETATE TETRAHYDRATE; MANGANESE CARBONATE; MERCURY; SODIUM SALICYLATE; SALICYLIC ACID; ALLYLTHIOUREA; THYROID, UNSPECIFIED
Strength	10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10
Strength Unit	[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL